A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530082



Internal ID20903443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3547016..3559210hg38UCSC Ensembl
chr19:3547014..3559208hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812195
hg1912195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046289
Samples
Known GenesMFSD12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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